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X-WR-CALDESC:Events for Novatek International
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DTSTART;TZID=UTC:20220427T080000
DTEND;TZID=UTC:20220429T170000
DTSTAMP:20260530T042752
CREATED:20220107T001505Z
LAST-MODIFIED:20220112T000417Z
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SUMMARY:HYBRID CONFERENCE & SPEAKER: KENX Cleanroom Validation\, Disinfection & EM
DESCRIPTION:SAVE $200 off your registration with CODE: Novatek200 \nWith the impending changes of Annex 1 as it applies the sterile environment and FDA’s Quality Consideration in Non-Sterile Drug Manufacturing Draft Guidance\, the time has never been greater to ensure you have procedures mastered to comply with regulatory authorities. KENX’s hybrid conference showcases those paving the way in best practices in cleanroom qualification\, disinfection\, contamination control\, environmental monitoring and more. As a bonus\, the event is co-located with Cleaning Validation and Critical Cleaning Processes and has over 40 tutorials to enhance your professional development. \nJoin KENX at industry’s cleanroom validation event of the year! Whether you’re in QA\, validation\, or engineering; a novice or advanced professional; or\, attending in-person or online\, this is your chance to network with over 200 of like-minded colleagues in the FDA-regulated environment. \nNovatek Speaker Session: \nTrending as part of a contamination control strategy  \nSusan Cleary B.CS\, EMBA – Direct Product Development\, Novatek International \n\nOverview on regulations and guidelines on EM data analysis\nUnderstand EM Trending Requirements\nLearn How to Trend & Analyze Environmental Monitoring Data\nConsiderations for EM data analysis using computerized systems\n\nTakeaway Tools \n\nExample Trend Reports\nRoot cause assessment data fields list\nTrending requirements examples for on demand\, weekly\, monthly\, quarterly\, and annual review
URL:https://ntint.com/event/hybrid-conference-kenx-cleanroom-validation-disinfection-em/
CATEGORIES:Conference,Virtual Conference
ATTACH;FMTTYPE=image/png:https://ntint.com/wp-content/uploads/2016/05/novatek-international-event.png
ORGANIZER;CN="KENX":MAILTO:info@kenx.org
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BEGIN:VEVENT
DTSTART;TZID=UTC:20220328T080000
DTEND;TZID=UTC:20220330T170000
DTSTAMP:20260530T042752
CREATED:20220107T002013Z
LAST-MODIFIED:20220112T000204Z
UID:18745-1648454400-1648659600@ntint.com
SUMMARY:HYBRID CONFERENCE & SPEAKER: KENX Validation University
DESCRIPTION:SAVE $200 off your registration with CODE: Novatek200 \n55 Tutorials Overflowing with Rich Content and Tangible Takeaways for the CQV Universe\nFacility Commissioning & Equipment Qualification\n\nImplement a Risk-based Verification Strategy\nDesign a Risk-based IQ\, OQ\, and PQ Approach\nManage Process Validation Tech Transfers\nQualify Critical Utility Systems – HVAC\, Water and Gas\n\nProcess Validation\n\nLearn How To Use Statistics in Validation – Statistics for Non-Statisticians\nImplement a 3-Stage Process Validation Approach\nMaster the Validation Master Plan (VMP)\nConduct Risk-based Continued Process Verfications\n\n Cleaning Validation\n\nUnderstand Key Elements to a Successful Program\nEstablish Cleaning Residue Limits and Acceptance Criteria\nEstablishing Bioburden and Endotoxin limits for Sterile and Non-sterile Products and Processes\nReceive a Cleaning Validation Assessment Checklist Example\n\n Computer System Validation\n\nStay up to speed with FDA’s Computer Software Assurance proposed draft\nImplement a Risk-Based CSV Program Enterprise-Wide\nDevelop and Validate SAAS\, IAAS\, and Other Software Programs\nQualify Network Infrastructure and Cloud Environments\n\n\nPersonnel In The Following Environments Should Attend:\n\nValidation\nQA/QC\nEngineering\nC&Q\nRegulatory and Compliance\nFacility Management\nManufacturing\nLaboratory
URL:https://ntint.com/event/hybrid-conference-speaker-kenx-validation-university/
CATEGORIES:Conference,Virtual Conference
ATTACH;FMTTYPE=image/png:https://ntint.com/wp-content/uploads/2016/05/novatek-international-event.png
ORGANIZER;CN="KENX":MAILTO:info@kenx.org
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